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Odu GmbH & Co. KG

FDA import alert and refusal historyMuhldorf a. Inn, GermanyFEI 3012975711

Recorded by FDA as ODU GMBH & CO. KG

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Example subjectOdu GmbH & Co. K added to Import Alert 16-129 (red list)

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As of October 26, 2026, Odu GmbH & Co. KG is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on December 10, 2018, most often for required label information not in english (NO ENGLISH).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Other bakery products, n.e.c. · NO ENGLISH
Last warning letter
None found
Last inspection
None on record

Every FDA record for Odu GmbH & Co. KG

1 record, newest first. Each line links to the FDA page it came from.

2018

  1. Import refusal
    Refused, Other bakery products, n.e.c.NO ENGLISHEntry SCS-2275820-6
    Source

Refusal charges, in plain English

  • NO ENGLISH1 refused line

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

Questions about Odu GmbH & Co. KG

Is Odu GmbH & Co. KG on an FDA import alert?
No listing for Odu GmbH & Co. KG appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Germany page.
Has FDA refused shipments from Odu GmbH & Co. KG?
Yes. FDA refused 1 shipment line from Odu GmbH & Co. KG on December 10, 2018. The most recent, on December 10, 2018, was other bakery products, n.e.c., charged as NO ENGLISH (required label information not in english).
Why did FDA refuse Odu GmbH & Co. KG's shipments?
The most frequent charge is NO ENGLISH (required label information not in english, 1 line).
What is Odu GmbH & Co. KG's FEI number?
Odu GmbH & Co. KG's FDA Establishment Identifier (FEI) is 3012975711.

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Example subjectOdu GmbH & Co. K added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.